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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Tick Salivary Compounds for Targeted Immunomodulatory Therapy

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Author(s):
Aounallah, Hajer [1, 2] ; Bensaoud, Chaima [3] ; M'ghirbi, Youmna [1] ; Faria, Fernanda [2] ; Chmelar, Jindrich [4] ; Kotsyfakis, Michail [3, 4]
Total Authors: 6
Affiliation:
[1] Univ Tunis El Manar, Serv Entomol Med, LR19IPTX, Inst Pasteur Tunis, Tunis - Tunisia
[2] Inst Butantan, Innovat & Dev Ctr, Innovat & Dev Lab, Sao Paulo - Brazil
[3] Acad Sci, Biol Ctr, Inst Parasitol, Ceske Budejovice - Czech Republic
[4] Univ South Bohemia Ceske Budejovice, Fac Sci, Dept Med Biol, Ceske Budejovice - Czech Republic
Total Affiliations: 4
Document type: Review article
Source: FRONTIERS IN IMMUNOLOGY; v. 11, SEP 23 2020.
Web of Science Citations: 0
Abstract

Immunodeficiency disorders and autoimmune diseases are common, but a lack of effective targeted drugs and the side-effects of existing drugs have stimulated interest in finding therapeutic alternatives. Naturally derived substances are a recognized source of novel drugs, and tick saliva is increasingly recognized as a rich source of bioactive molecules with specific functions. Ticks use their saliva to overcome the innate and adaptive host immune systems. Their saliva is a rich cocktail of molecules including proteins, peptides, lipid derivatives, and recently discovered non-coding RNAs that inhibit or modulate vertebrate immune reactions. A number of tick saliva and/or salivary gland molecules have been characterized and shown to be promising candidates for drug development for vertebrate immune diseases. However, further validation of these molecules at the molecular, cellular, and organism levels is now required to progress lead candidates to clinical testing. In this paper, we review the data on the immuno-pharmacological aspects of tick salivary compounds characterizedin vitroand/orin vivoand present recent findings on non-coding RNAs that might be exploitable as immunomodulatory therapies. (AU)

FAPESP's process: 13/07467-1 - CeTICS - Center of Toxins, Immune-Response and Cell Signaling
Grantee:Hugo Aguirre Armelin
Support Opportunities: Research Grants - Research, Innovation and Dissemination Centers - RIDC